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nsv6716115

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:418

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Submitted genomic11,013,481-11,013,898Question Mark
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):11,055,167-11,055,584Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6716115Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,013,48111,013,898
    nsv6716115RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,055,16711,055,584

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18667247duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18667247Submitted genomicNC_000003.12:g.110
    13481_11013898dup
    GRCh38 (hg38)NC_000003.12Chr311,013,48111,013,898
    nssv18667247RemappedPerfectNC_000003.11:g.110
    55167_11055584dup
    GRCh37.p13First PassNC_000003.11Chr311,055,16711,055,584

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv186672474e-061244414
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